A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140603



Internal ID21419214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119619754..119619754hg38UCSC Ensembl
chr7:119259808..119259808hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637924
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140603
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer